Variant report

Variant	rs9809570
Chromosome Location	chr3:194879917-194879918
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:194879007..194881053-chr3:194979480..194982311,2	K562	blood:
2	chr3:194879313..194881021-chr3:194894855..194897283,2	MCF-7	breast:
3	chr3:194879840..194881692-chr3:194900733..194902679,2	K562	blood:
4	chr3:194879677..194882151-chr3:194884432..194886543,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000173950	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10433328	0.89[ASN][1000 genomes]
rs10433329	0.93[ASN][1000 genomes]
rs10433330	0.93[ASN][1000 genomes]
rs10933700	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10933701	0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12491661	0.90[ASN][1000 genomes]
rs12491663	0.84[ASN][1000 genomes]
rs2004553	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2088040	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2088041	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2410844	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2410846	0.82[ASN][1000 genomes]
rs28613110	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4677662	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4677811	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4677814	0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs59556963	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59834989	0.88[AMR][1000 genomes]
rs60528401	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6437460	0.90[ASN][1000 genomes]
rs6799346	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73206648	0.88[ASN][1000 genomes]
rs73206650	0.88[ASN][1000 genomes]
rs73206651	0.93[ASN][1000 genomes]
rs7628775	0.85[ASN][1000 genomes]
rs7637593	0.85[ASN][1000 genomes]
rs7653355	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs903309	0.88[ASN][1000 genomes]
rs903311	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9824084	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9825521	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007697	chr3:194554814-195009930	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv536873	chr3:194554814-195009930	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
3	nsv997779	chr3:194687093-194885936	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
4	nsv536874	chr3:194687093-194885936	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1009796	chr3:194737333-195124248	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
6	nsv1012592	chr3:194814446-194931562	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
7	nsv536875	chr3:194814446-194931562	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
8	nsv1001492	chr3:194814990-194935397	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
9	nsv461126	chr3:194817484-194961888	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
10	nsv592981	chr3:194817484-194961888	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
11	nsv878137	chr3:194822098-194900432	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
12	nsv461127	chr3:194833940-194934634	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
13	nsv592982	chr3:194833940-194934634	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
14	nsv1014826	chr3:194834615-195631793	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
15	nsv536876	chr3:194834615-195631793	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
16	nsv533904	chr3:194868329-195438728	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
17	nsv1009120	chr3:194874494-194974672	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
18	nsv1010168	chr3:194874494-195135790	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
19	nsv536877	chr3:194874494-195135790	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
20	nsv997956	chr3:194879534-195087539	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
21	nsv536878	chr3:194879534-195087539	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:194861000-194881000	Weak transcription	Hela-S3	cervix
2	chr3:194862400-194897800	Weak transcription	Dnd41	blood
3	chr3:194868800-194885400	Enhancers	Fetal Muscle Leg	muscle
4	chr3:194871000-194880800	Enhancers	HUVEC	blood vessel
5	chr3:194871400-194887400	Enhancers	Primary hematopoietic stem cells	blood
6	chr3:194871600-194881200	Weak transcription	Liver	Liver
7	chr3:194871800-194882800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr3:194872000-194882800	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr3:194872000-194883000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr3:194872000-194883000	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr3:194873000-194884400	Enhancers	Primary B cells from peripheral blood	blood
12	chr3:194873000-194884600	Enhancers	Fetal Thymus	thymus
13	chr3:194874000-194889800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr3:194876000-194880200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:194876200-194880200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr3:194876200-194880200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr3:194876200-194880200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr3:194876200-194880200	Weak transcription	HSMMtube	muscle
19	chr3:194876200-194881000	Enhancers	HepG2	liver
20	chr3:194876400-194880000	Weak transcription	Placenta	Placenta
21	chr3:194876400-194881200	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr3:194876600-194880000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr3:194876600-194880200	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr3:194876600-194880400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr3:194876600-194880800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr3:194876600-194881000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:194876600-194893000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr3:194876800-194880000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr3:194876800-194880000	Weak transcription	Osteobl	bone
30	chr3:194876800-194880200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr3:194876800-194880200	Weak transcription	Fetal Kidney	kidney
32	chr3:194876800-194880200	Weak transcription	K562	blood
33	chr3:194876800-194880800	Weak transcription	HSMM	muscle
34	chr3:194876800-194881400	Weak transcription	Esophagus	oesophagus
35	chr3:194876800-194893800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr3:194877000-194880000	Weak transcription	Small Intestine	intestine
37	chr3:194877000-194880200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr3:194877000-194880200	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr3:194877000-194880800	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr3:194877000-194881000	Weak transcription	NHEK	skin
41	chr3:194877000-194881400	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr3:194877000-194881400	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr3:194877200-194881200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr3:194877200-194881200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr3:194877200-194881200	Weak transcription	Stomach Mucosa	stomach
46	chr3:194877200-194884200	Weak transcription	Gastric	stomach
47	chr3:194877200-194891200	Weak transcription	Psoas Muscle	Psoas
48	chr3:194877400-194880000	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr3:194877400-194880000	Weak transcription	Lung	lung
50	chr3:194877400-194880000	Weak transcription	Right Atrium	heart

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